Osseointegrated Prosthetic Implants for People With Lower-Limb Amputation: A Health Technology Assessment.

Q1 Medicine
Ontario Health Technology Assessment Series Pub Date : 2019-12-12 eCollection Date: 2019-01-01
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Our analysis included an evaluation of effectiveness, safety, cost-effectiveness, the budget impact of publicly funding osseointegrated prosthetic implants, and patient preferences and values.</p><p><strong>Methods: </strong>We performed a systematic literature search of the clinical evidence on the safety and effectiveness of the latest iterations of three implant systems: the Osseointegrated Prostheses for the Rehabilitation of Amputees (OPRA) Implant System, the Endo-Exo-Femur-Prosthesis, and the Osseointegration Group of Australia-Osseointegration Prosthetic Limb (OGAP-OPL). We assessed the risk of bias of individual studies and determined the quality of the body of evidence according to the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) Working Group criteria. We performed a systematic economic literature search and conducted a cost-utility analysis with a lifetime horizon from a public payer perspective. We also analyzed the net budget impact of publicly funding osseointegrated prosthetic implants in Ontario. To contextualize the potential value of osseointegrated prosthetic implants, we spoke with people with lower-limb amputations.</p><p><strong>Results: </strong>We included nine studies in the clinical evidence review. All studies included patients with above-the-knee amputation who underwent two-stage surgery and mostly had short-term follow-up. With osseointegrated prosthetic implants, scores for functional outcomes improved significantly as measured by 6-Minute Walk Test (6MWT), Timed Up and Go (TUG) test, and Questionnaire for Persons with a Transfemoral Amputation (Q-TFA). The scores for quality of life measured by SF-36 showed significant improvement in the physical component summary but a nonsignificant decline for the mental component summary. The most frequently seen adverse event was superficial infection, occurring in about half of patients in some studies. 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引用次数: 0

Abstract

Background: Osseointegrated prosthetic implants are biocompatible metal devices that are inserted into the residual bone to integrate with the bone and attach to the external prosthesis, eliminating the need for socket prostheses and the problems that may accompany their use. We conducted a health technology assessment of osseointegrated prosthetic implants, compared with conventional socket prostheses, for people with lower-limb amputation who experience chronic problems with their prosthetic socket, leading to prosthesis intolerance and reduced mobility. Our analysis included an evaluation of effectiveness, safety, cost-effectiveness, the budget impact of publicly funding osseointegrated prosthetic implants, and patient preferences and values.

Methods: We performed a systematic literature search of the clinical evidence on the safety and effectiveness of the latest iterations of three implant systems: the Osseointegrated Prostheses for the Rehabilitation of Amputees (OPRA) Implant System, the Endo-Exo-Femur-Prosthesis, and the Osseointegration Group of Australia-Osseointegration Prosthetic Limb (OGAP-OPL). We assessed the risk of bias of individual studies and determined the quality of the body of evidence according to the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) Working Group criteria. We performed a systematic economic literature search and conducted a cost-utility analysis with a lifetime horizon from a public payer perspective. We also analyzed the net budget impact of publicly funding osseointegrated prosthetic implants in Ontario. To contextualize the potential value of osseointegrated prosthetic implants, we spoke with people with lower-limb amputations.

Results: We included nine studies in the clinical evidence review. All studies included patients with above-the-knee amputation who underwent two-stage surgery and mostly had short-term follow-up. With osseointegrated prosthetic implants, scores for functional outcomes improved significantly as measured by 6-Minute Walk Test (6MWT), Timed Up and Go (TUG) test, and Questionnaire for Persons with a Transfemoral Amputation (Q-TFA). The scores for quality of life measured by SF-36 showed significant improvement in the physical component summary but a nonsignificant decline for the mental component summary. The most frequently seen adverse event was superficial infection, occurring in about half of patients in some studies. Deep or bone infection was a serious adverse event, with variable rates among the studies depending on the length of follow-up. The treatment of deep or bone infection required long-term antibiotic use, surgical debridement, revision surgery, and implant extraction in some cases. Other adverse events included femoral bone fracture, implant breakage, issues with extramedullary parts that required replacement, and implant removal. Our assessment of the quality of the clinical evidence according to the GRADE criteria found low certainty in terms of improvement in functional outcomes, low certainty for quality of life, and high certainty of an increase in adverse events; all findings compared receiving an osseointegrated prosthetic implant with not receiving an osseointegrated prosthetic implant.In our economic model, osseointegrated prosthetic implants were found to be more effective and more expensive than having people remain users of an uncomfortable socket prosthesis. Our best estimate of the incremental cost-effectiveness ratio (ICER) for osseointegration, compared with an uncomfortable socket, was $94,987 per quality-adjusted life-year (QALY) gained. The probability of osseointegration being cost-effective was 54.2% at a willingness-to-pay value of $100,000 per QALY gained. The annual net budget impact of publicly funding osseointegrated prosthetic implants in Ontario over the next 5 years, for a small population of eligible candidates, would range from $1.5 million in year 1 to $0.6 million in year 5, for a 5-year total of $5.3 million.We interviewed 13 people with a lower-limb amputation; nine had experience with both a conventional socket prosthesis and an osseointegrated prosthetic implant, three had experience with a conventional socket prosthesis only, and one had only recently undergone amputation and had not yet chosen a prosthesis. People who had received an osseointegrated prosthetic implant said they had better mobility and quality of life than before receiving this implant but had concerns about the ongoing risk of infection and potential for problems with implant maintenance. People using a conventional socket prosthesis said cost was the only factor preventing them from undergoing an osseointegration procedure.

Conclusions: In the studies included in the clinical evidence review, most people who received osseointegrated prosthetic implants were followed for only a few years. Studies showed that functional outcomes and physical ability improved with osseointegrated prosthetic implants (GRADE: Low), but there was uncertainty about the impact of these implants on people's emotional health (GRADE: Low). Osseointegrated prosthetic implants can lead to serious adverse events such as bone infection and bone fracture in some patients, which may require additional surgeries (GRADE: High). The reference case of the primary economic evaluation represented a conservative estimate of cost-effectiveness and found osseointegration may be cost-effective, but there is a large degree of uncertainty given parameter uncertainty and the need to use proxy costs. Scenario analyses explored potential variations in approaches to modelling and parameter selection. Qualitative interviews with people with a lower-limb amputation and caregivers underscored the challenges of conventional socket prostheses, but cost remains an important barrier to pursuing osseointegrated prosthetic implantation.

下肢截肢患者骨整合假体植入:健康技术评估
背景:骨整合假体植入物是一种生物相容性的金属装置,可插入残骨中与骨融合并附着于外部假体,从而消除了对窝形假体的需求及其可能伴随使用的问题。我们对下肢截肢患者进行了骨整合假体植入物的健康技术评估,与传统的假体窝相比,这些患者的假体窝存在慢性问题,导致假体耐受不良和活动能力降低。我们的分析包括有效性、安全性、成本效益、公共资助骨整合假体植入的预算影响以及患者的偏好和价值观的评估。方法:我们系统地检索了最新迭代的三种种植系统的临床证据:用于截肢者康复的骨整合假体(OPRA)种植系统、内-外-股骨假体和澳大利亚骨整合假肢组(OGAP-OPL)。我们评估了个别研究的偏倚风险,并根据建议分级评估、发展和评价(GRADE)工作组的标准确定了证据体的质量。我们进行了系统的经济文献检索,并从公共付款人的角度进行了终身成本效用分析。我们还分析了安大略省公共资助骨整合假体植入的净预算影响。为了了解骨整合假体植入物的潜在价值,我们与下肢截肢患者进行了交谈。结果:我们在临床证据综述中纳入了9项研究。所有的研究都包括了接受了两阶段手术的膝盖以上截肢患者,他们大多有短期随访。使用骨整合假体植入物,通过6分钟步行测试(6MWT)、计时起身和行走(TUG)测试和经股截肢者问卷(Q-TFA)测量功能结果得分显着改善。SF-36测量的生活质量得分显示身体成分总结有显著改善,但精神成分总结没有显著下降。最常见的不良事件是表面感染,在一些研究中约有一半的患者发生。深度或骨骼感染是一个严重的不良事件,根据随访时间的长短,不同研究的发生率不同。深度或骨感染的治疗需要长期使用抗生素、外科清创、翻修手术,在某些情况下还需要拔出种植体。其他不良事件包括股骨骨折、植入物断裂、需要更换的髓外部分问题和植入物移除。我们根据GRADE标准对临床证据质量的评估发现,功能结局改善的确定性较低,生活质量的确定性较低,不良事件增加的确定性较高;所有结果都比较了接受骨整合假体种植体和未接受骨整合假体种植体的情况。在我们的经济模型中,骨整合假体植入物被发现比让人们继续使用不舒服的插座假体更有效,也更昂贵。我们对骨整合的增量成本效益比(ICER)的最佳估计,与不舒服的套槽相比,每获得质量调整生命年(QALY)为94,987美元。骨整合具有成本效益的概率为54.2%,每个获得的QALY的支付意愿价值为100,000美元。未来5年,安大略省骨整合假体植入的年度净预算影响将从第一年的150万美元到第五年的60万美元不等,总共为530万美元。我们采访了13个下肢截肢的人;其中9名患者同时使用过传统的假体和骨整合假体,3名患者仅使用过传统的假体,1名患者最近才接受过截肢手术,尚未选择假体。接受骨整合假体植入的患者表示,与接受植入前相比,他们的活动能力和生活质量都有所改善,但他们仍担心感染的风险和植入物维护的潜在问题。使用传统假体的人说,成本是阻止他们接受骨整合手术的唯一因素。结论:在临床证据综述中纳入的研究中,大多数接受骨整合假体植入的患者仅随访了几年。 研究表明,骨整合假体植入物改善了功能结局和身体能力(GRADE: Low),但这些植入物对人们情绪健康的影响尚不确定(GRADE: Low)。骨整合假体植入物可能导致严重的不良事件,如骨感染和骨折,这可能需要额外的手术(GRADE:高)。初步经济评估的参考案例代表了对成本效益的保守估计,并发现骨整合可能具有成本效益,但考虑到参数的不确定性和使用代理成本的必要性,存在很大程度的不确定性。情景分析探讨了建模和参数选择方法的潜在变化。对下肢截肢患者和护理人员的定性访谈强调了传统的窝式假体的挑战,但成本仍然是追求骨整合假体植入的重要障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Ontario Health Technology Assessment Series
Ontario Health Technology Assessment Series Medicine-Medicine (miscellaneous)
CiteScore
4.60
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